Pregled bibliografske jedinice broj: 734183
Epidemiology of multiple congenital anomalies in Europe : A EUROCAT population-based registry study
Epidemiology of multiple congenital anomalies in Europe : A EUROCAT population-based registry study // Birth defects research. Part A. Clinical and molecular teratology, 100 (2014), 4; 270-276 doi:10.1002/bdra.23240 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 734183 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Epidemiology of multiple congenital anomalies in Europe : A EUROCAT population-based registry study
Autori
Calzolari, E. ; Barišić, Ingeborg ; Loane, M. ; Morris, J. ; Wellesley, D. ; Dolk, H. ; Addor, M.C. ; Arriola, L. ; Bianchi, F. ; Neville, A.J. ; Budd, J.L. ; Klungsoyr, K. ; Khoshnood, B. ; McDonnell, B. ; Nelen, V. ; Queisser-Luft, A. ; Rankin, J. ; Rissmann, A. ; Rounding, C. ; Tucker, D. ; Verellen-Dumoulin, C. ; de Walle, H. ; Garne, E.
Izvornik
Birth defects research. Part A. Clinical and molecular teratology (1542-0752) 100
(2014), 4;
270-276
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Epidemiology ; Multiple congenital anomalies ; Classification ; Prevalence ; Prenatal diagnosis
Sažetak
This study describes the prevalence, associated anomalies, and demographic characteristics of cases of multiple congenital anomalies (MCA) in 19 population-based European registries (EUROCAT) covering 959, 446 births in 2004 and 2010. EUROCAT implemented a computer algorithm for classification of congenital anomaly cases followed by manual review of potential MCA cases by geneticists. MCA cases are defined as cases with two or more major anomalies of different organ systems, excluding sequences, chromosomal and monogenic syndromes. The combination of an epidemiological and clinical approach for classification of cases has improved the quality and accuracy of the MCA data. Total prevalence of MCA cases was 15.8 per 10, 000 births. Fetal deaths and termination of pregnancy were significantly more frequent in MCA cases compared with isolated cases (p < 0.001) and MCA cases were more frequently prenatally diagnosed (p < 0.001). Live born infants with MCA were more often born preterm (p < 0.01) and with birth weight < 2500 grams (p < 0.01). Respiratory and ear, face, and neck anomalies were the most likely to occur with other anomalies (34% and 32%) and congenital heart defects and limb anomalies were the least likely to occur with other anomalies (13%) (p < 0.01). However, due to their high prevalence, congenital heart defects were present in half of all MCA cases. Among males with MCA, the frequency of genital anomalies was significantly greater than the frequency of genital anomalies among females with MCA (p < 0.001). Although rare, MCA cases are an important public health issue, because of their severity. The EUROCAT database of MCA cases will allow future investigation on the epidemiology of these conditions and related clinical and diagnostic problems
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
MZOS-072-1083107-0365 - Istraživanje epidemiologijskih i genetičkih osnova prirođenih mana (Barišić, Ingeborg, MZOS ) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta
Profili:
Ingeborg Barišić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE